ClinVar Miner

Submissions for variant NM_018075.5(ANO10):c.218G>A (p.Gly73Asp)

dbSNP: rs2149481812
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein RCV001528140 SCV001739350 uncertain significance Autosomal recessive spinocerebellar ataxia 10 2021-05-20 no assertion criteria provided clinical testing

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